A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749155



Internal ID20525184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63880097..63880217hg38UCSC Ensembl
chr20:62511450..62511570hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284207
Samples
Known GenesTPD52L2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749155
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer